Fmr1 exon 14 skipping in late embryonic development of the rat forebrain

BACKGROUND: Fragile X syndrome, the major cause of inherited intellectual disability among men, is due to deficiency of the synaptic functional regulator FMR1 protein (FMRP), encoded by the FMRP translational regulator 1 (FMR1) gene. FMR1 alternative splicing produces distinct transcripts that may c...

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Detalles Bibliográficos
Autores principales: Corrêa-Velloso, Juliana C., Linardi, Alessandra M., Glaser, Talita, Velloso, Fernando J., Rivas, Maria P., Leite, Renata E P., Grinberg, Lea T., Ulrich, Henning, Akins, Michael R., Chiavegatto, Silvana, Haddad, Luciana A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9158170/
https://www.ncbi.nlm.nih.gov/pubmed/35641906
http://dx.doi.org/10.1186/s12868-022-00711-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9158170/
https://www.ncbi.nlm.nih.gov/pubmed/35641906
http://dx.doi.org/10.1186/s12868-022-00711-1

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